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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713376Generated: November 2, 2026

Carbon tetrabromide → 1-(3-Bromomethyl-4-trityloxybutyl)-1H-pyrimidine-2,4-dione

https://huagongshe.com/reaction/1713376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(3-Hydroxymethyl-4-trityloxybutyl)-1H-pyrimidine-2,4-dioneHCID 59463757—
SolventDimethylformamideHCID 6228—
Product1-(3-Bromomethyl-4-trityloxybutyl)-1H-pyrimidine-2,4-dioneHCID 5946376058%

Reaction Steps

To a solution of compound 36 (33 g, 0.073 mol) in dry DMF (200 mL) was added triphenylphosphine (29 g, 0.11 mol) with vigorous stirring at RT. The reaction mixture was cooled to 0° C., added CBr4 (36 g, 0.11 mol) portion wise over a period of 30 min and allowed to stir at RT for 24 h. The reaction mixture was cooled to 0° C., added saturated NaHCO3 solution (100 mL) and extracted with ethyl acetate (4×150 mL). The combined organic layer was dried, concentrated under vacuum and the crude product was purified by column chromatography on silica gel (50% ethyl acetate in hexane) to give the title compound (22 g, 57%). TLC: 100% EtOAc, Rf=0.7

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795270B2
Source datasetuspto-grants-2010_09
ORD IDord-26c10fc73c7c4fbc804e6a548f6c3cd3
Source noteuspto-grants-2010_09